S()-2-AMINO-1-PROPANOL-3,3,3-D3

AR

Reagent Code: #92550
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CAS Number 352438-84-7

science Other reagents with same CAS 352438-84-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 78.13 g/mol
Formula C₃H₆D₃NO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of deuterated pharmaceuticals and biochemicals, where it serves as a chiral building block. Its deuterium labeling makes it valuable in isotopic labeling studies, particularly in NMR spectroscopy and mass spectrometry, to track molecular pathways and mechanisms in drug metabolism research. Additionally, it is employed in the development of deuterated analogs of active pharmaceutical ingredients to enhance their stability and pharmacokinetic properties. Its chiral nature also makes it useful in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,220.00

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S()-2-AMINO-1-PROPANOL-3,3,3-D3
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This compound is primarily utilized in the synthesis of deuterated pharmaceuticals and biochemicals, where it serves as a chiral building block. Its deuterium labeling makes it valuable in isotopic labeling studies, particularly in NMR spectroscopy and mass spectrometry, to track molecular pathways and mechanisms in drug metabolism research. Additionally, it is employed in the development of deuterated analogs of active pharmaceutical ingredients to enhance their stability and pharmacokinetic properties.

This compound is primarily utilized in the synthesis of deuterated pharmaceuticals and biochemicals, where it serves as a chiral building block. Its deuterium labeling makes it valuable in isotopic labeling studies, particularly in NMR spectroscopy and mass spectrometry, to track molecular pathways and mechanisms in drug metabolism research. Additionally, it is employed in the development of deuterated analogs of active pharmaceutical ingredients to enhance their stability and pharmacokinetic properties. Its chiral nature also makes it useful in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.

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